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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840417Generated: October 30, 2026

3-Cyano-N-[(2S)-2-(3,4-dichlorophenyl)-4-oxobutyl)-N-methyl-1-naphthamide → N-[2-(S)-(3,4-Dichlorophenyl)-4-[4-[2-(methylsulfonyl)-4-methoxyphenyl]-1-piperidinyl]-butyl]-N-methyl-3-cyano-1-naphthamide Hydrochloride

https://huagongshe.com/reaction/840417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyano-N-[(2S)-2-(3,4-dichlorophenyl)-4-oxobutyl)-N-methyl-1-naphthamideHCID 18715645—
Reactant4-(2-Methylsulfonyl-4-methoxyphenyl)piperidineHCID 22622334—
ProductN-[2-(S)-(3,4-Dichlorophenyl)-4-[4-[2-(methylsulfonyl)-4-methoxyphenyl]-1-piperidinyl]-butyl]-N-methyl-3-cyano-1-naphthamide HydrochlorideHCID 18715621—

Reaction Steps

Using standard reductive amination conditions N-[2-(S)-(3,4-dichlorophenyl)-4-oxobutyl]-N-methyl-3-cyano-1-naphthamide (0.130 g) was reacted with 4-(2-methylsulfonyl-4-methoxyphenyl)piperidine (0.082 g) and the product (0.074 g) was converted to the hydrochloride salt. MS m/z 678 (M+H). 1H NMR (DMSO-d6) δ 10.57 (m, 1H), 8.62 (m, 1H), 8.10 (m, 1H), 7.95-7.00 (m, 10H), 3.83 (s, 3H), 3.32 (s, 3H), 3.64-1.65 (m, 19H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365602B1
Source datasetuspto-grants-2002_04
ORD IDord-0252e0cc72e6406c8d3803d75bad39a8
Source noteuspto-grants-2002_04